Taiwan FDA registration fed91e2af0c39ec3498cd9d1f4598a23

"Hankil" Orthopedic manual surgical instrument (Non-Sterile)

TW: "漢奇" 手動式骨科手術器械 (未滅菌)

Taiwan·Risk Class 1·MD·HANKIL TECH MEDICAL CO., LTD.·Registered Aug 12, 2016 – Aug 12, 2026Active

Registration details

Analysis ID: fed91e2af0c39ec3498cd9d1f4598a23
License Form: Ministry of Health Medical Device Import No. 016892
Customs Code: DHA09401689207

Company information

Manufacturer: HANKIL TECH MEDICAL CO., LTD.
Manufacturer Country: Korea, Republic of
Authorized Representative: DE LI BIOTECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
Product Type (Level 1): N Orthopedic devices
Product Type (Level 2): N4540 Manual osteologic surgery instrument
Import Information: Imported from abroad

Dates and status

Registration Date: Aug 12, 2016
Expiry Date: Aug 12, 2026

About this record

Access comprehensive regulatory information for "Hankil" Orthopedic manual surgical instrument (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fed91e2af0c39ec3498cd9d1f4598a23 and manufactured by HANKIL TECH MEDICAL CO., LTD.. The authorized representative in Taiwan is DE LI BIOTECHNOLOGY CO., LTD..

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